Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction. - Wikidata - awgldk - TriplyDB

Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction.

Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction.

http://www.wikidata.org/entity/Q34103271

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Gender differences in genetic risk profiles for cardiovascular disease Assessing the impact of population stratification on genetic association studies Biophysical characterization of the signature domains of thrombospondin-4 and thrombospondin-2 Mechanism and effect of thrombospondin-4 polymorphisms on neutrophil function Influences of the N700S Thrombospondin-1 Polymorphism on Protein Structure and Stability Genetics of the acute coronary syndrome Coronary collateral growth--back to the future The gene expression fingerprint of human heart failure.Phylogenomic analysis of vertebrate thrombospondins reveals fish-specific paralogues, ancestral gene relationships and a tetrapod innovation.Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality.Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction.Genetic loci that control the size of laser-induced choroidal neovascularization Lack of MEF2A mutations in coronary artery disease.A hidden two-locus disease association pattern in genome-wide association studies Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis.Control of organization and function of muscle and tendon by thrombospondin-4.A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study A polymorphism in thrombospondin-1 associated with familial premature coronary heart disease causes a local change in conformation of the Ca2+-binding repeats.Polymorphism in THBS1 gene is associated with post-refractive surgery chronic ocular surface inflammation.Thrombospondin-4 regulates vascular inflammation and atherogenesis.Variants associated with common disease are not unusually differentiated in frequency across populations.Molecular and functional differences induced in thrombospondin-1 by the single nucleotide polymorphism associated with the risk of premature, familial myocardial infarction.Plasminogen activator inhibitor-2 polymorphism associates with recurrent coronary event risk in patients with high HDL and C-reactive protein levels.Genetic testing for coronary heart disease: the approaching frontier.Thrombospondin-1 up-regulates expression of cell adhesion molecules and promotes monocyte binding to endothelium.Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes.Genetic evaluation for coronary artery disease.The thrombospondins.Matricellular proteins in cardiac adaptation and disease.Gender differences in the prevalence, severity, and composition of coronary artery disease in the young: a study of 1635 individuals undergoing coronary CT angiography from the prospective, multinational confirm registry Association of genetic variants with coronary artery disease and ischemic stroke in a longitudinal population-based genetic epidemiological study Higher plasma thrombospondin-1 levels in patients with coronary artery disease and diabetes mellitus.Intermolecular interactions of thrombospondins drive their accumulation in extracellular matrix.The thrombospondin-1 N700S polymorphism is associated with early myocardial infarction without altering von Willebrand factor multimer size Distinctive Clinical Profile of Blacks Versus Whites Presenting With Sudden Cardiac Arrest.Molecular aspects of thrombosis and antithrombotic drugs.Proangiogenic Properties of Thrombospondin-4.Personalized medicine in cardiovascular diseases.Association between variations in coagulation system genes and carotid plaque.Function-blocking antithrombospondin-1 monoclonal antibodies

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P2860

Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction.

http://www.wikidata.org/entity/Q34103271

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2001 nî lūn-bûn

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2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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Single nucleotide polymorphism ...... emature myocardial infarction.

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Single nucleotide polymorphism ...... emature myocardial infarction.

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Single nucleotide polymorphism ...... emature myocardial infarction.

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Single nucleotide polymorphism ...... emature myocardial infarction.

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